A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842096



Internal ID22025739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28765464..28765464hg38UCSC Ensembl
chr10:29054393..29054393hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842096
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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